Ondansetron
- Product NDC
- 71872-7162
- 11-digit product format
- 718727162
- Labeler code
- 71872
- Product ID
- 71872-7162_0cf7da8b-6f35-d806-e063-6394a90ad6d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ONDANSETRON
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA077548
- Marketing category
- ANDA
- Marketing start
- 2008-10-16
- Substance
- ONDANSETRON HYDROCHLORIDE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| NMH84OZK2B | ONDANSETRON HYDROCHLORIDE | 103639-04-9 | ONDANSETRON HYDROCHLORIDE |
| 4AF302ESOS | ONDANSETRON | 99614-02-5 | ONDANSETRON |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7162-1 | 71872716201 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7162-1) / 2 mL in 1 VIAL, SINGLE-DOSE | 2019-04-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ondansetron | Medical Purchasing Solutions, LLC | 2023-05-15 | HUMAN PRESCRIPTION DRUG LABEL | 6 |